Variant #0000976203 (NC_000004.11:g.169799389_169799391dup, NC_000004.11(NM_016081.3):c.1965-12684_1965-12682dup (PALLD))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.169799389_169799391dup
DNA change (hg38) -
Published as PALLD(NM_001166110.2):c.347_349dup (p.(Pro116dup))
ISCN -
DB-ID PALLD_000031
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PALLD NM_016081.3 -?/. - c.1965-12684_1965-12682dup r.(=) p.(=)


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